Krishna Kumar

Characterization of a distinct lethal arteriopathy syndrome in twenty-two infants associated with an identical, novel mutation in FBLN4 gene, confirms fibulin-4 as a critical determinant of human vascular elastogenesis

S. Menon, S. Nampoothiri, A. De Paepe, 2012, Orphanet Journal of Rare Diseases.

Neurological complications of congenital heart disease

Krishna Kumar, K. Kumar, 2000, Indian journal of pediatrics.

Repair of Congenital Heart Disease with Associated Pulmonary Hypertension in Children: What are the Minimal Investigative Procedures? Consensus Statement from the Congenital Heart Disease and Pediatric Task Forces, Pulmonary Vascular Research Institute (PVRI)

S. Harikrishnan, A. Mocumbi, R. Barst, 2014, Pulmonary circulation.

Starting and Operating a Public Cardiac Catheterization Laboratory in a Low Resource Setting: The Eight-Year Story of the Uganda Heart Institute Catheter Laboratory

C. Mondo, C. Longenecker, D. Simon, 2021, Global heart.